rs587776628

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587776628(A;A)

Make rs587776628(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

44823064

Gene

PTCH2

is a	snp
is	mentioned by
dbSNP	rs587776628
dbSNP (classic)	rs587776628
ClinGen	rs587776628
ebi	rs587776628
HLI	rs587776628
Exac	rs587776628
Gnomad	rs587776628
Varsome	rs587776628
LitVar	rs587776628
Map	rs587776628
PheGenI	rs587776628
Biobank	rs587776628
1000 genomes	rs587776628
hgdp	rs587776628
ensembl	rs587776628
geneview	rs587776628
scholar	rs587776628
google	rs587776628
pharmgkb	rs587776628
gwascentral	rs587776628
openSNP	rs587776628
23andMe	rs587776628
SNPshot	rs587776628
SNPdbe	rs587776628
MSV3d	rs587776628
GWAS Ctlg	rs587776628

Max Magnitude

0

ClinVar
Risk	rs587776628(A;A) Rs587776628(G;G)
Alt	rs587776628(A;A) Rs587776628(G;G)
Reference	Rs587776628(C;C)
Significance	Pathogenic
Disease	Basal cell carcinoma
Variation	info
Gene	PTCH2
CLNDBN	Basal cell carcinoma, somatic
Reversed	1
HGVS	NC_000001.10:g.45288736G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006521.5,